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Further Introduction of DNA Methylation (DNAm) Arrays in Regular Diagnostics

Methylation tests have been used for decades in regular DNA diagnostics focusing primarily on Imprinting disorders or specific loci annotated to specific disease associated gene promotors. With the introduction of DNA methylation (DNAm) arrays such as the Illumina Infinium HumanMethylation450 Beadch...

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Autores principales: Mannens, M. M. A. M., Lombardi, M. P., Alders, M., Henneman, P., Bliek, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9289263/
https://www.ncbi.nlm.nih.gov/pubmed/35860466
http://dx.doi.org/10.3389/fgene.2022.831452
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author Mannens, M. M. A. M.
Lombardi, M. P.
Alders, M.
Henneman, P.
Bliek, J.
author_facet Mannens, M. M. A. M.
Lombardi, M. P.
Alders, M.
Henneman, P.
Bliek, J.
author_sort Mannens, M. M. A. M.
collection PubMed
description Methylation tests have been used for decades in regular DNA diagnostics focusing primarily on Imprinting disorders or specific loci annotated to specific disease associated gene promotors. With the introduction of DNA methylation (DNAm) arrays such as the Illumina Infinium HumanMethylation450 Beadchip array or the Illumina Infinium Methylation EPIC Beadchip array (850 k), it has become feasible to study the epigenome in a timely and cost-effective way. This has led to new insights regarding the complexity of well-studied imprinting disorders such as the Beckwith Wiedemann syndrome, but it has also led to the introduction of tests such as EpiSign, implemented as a diagnostic test in which a single array experiment can be compared to databases with known episignatures of multiple genetic disorders, especially neurodevelopmental disorders. The successful use of such DNAm tests is rapidly expanding. More and more disorders are found to be associated with discrete episignatures which enables fast and definite diagnoses, as we have shown. The first examples of environmentally induced clinical disorders characterized by discrete aberrant DNAm are discussed underlining the broad application of DNAm testing in regular diagnostics. Here we discuss exemplary findings in our laboratory covering this broad range of applications and we discuss further use of DNAm tests in the near future.
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spelling pubmed-92892632022-07-19 Further Introduction of DNA Methylation (DNAm) Arrays in Regular Diagnostics Mannens, M. M. A. M. Lombardi, M. P. Alders, M. Henneman, P. Bliek, J. Front Genet Genetics Methylation tests have been used for decades in regular DNA diagnostics focusing primarily on Imprinting disorders or specific loci annotated to specific disease associated gene promotors. With the introduction of DNA methylation (DNAm) arrays such as the Illumina Infinium HumanMethylation450 Beadchip array or the Illumina Infinium Methylation EPIC Beadchip array (850 k), it has become feasible to study the epigenome in a timely and cost-effective way. This has led to new insights regarding the complexity of well-studied imprinting disorders such as the Beckwith Wiedemann syndrome, but it has also led to the introduction of tests such as EpiSign, implemented as a diagnostic test in which a single array experiment can be compared to databases with known episignatures of multiple genetic disorders, especially neurodevelopmental disorders. The successful use of such DNAm tests is rapidly expanding. More and more disorders are found to be associated with discrete episignatures which enables fast and definite diagnoses, as we have shown. The first examples of environmentally induced clinical disorders characterized by discrete aberrant DNAm are discussed underlining the broad application of DNAm testing in regular diagnostics. Here we discuss exemplary findings in our laboratory covering this broad range of applications and we discuss further use of DNAm tests in the near future. Frontiers Media S.A. 2022-07-04 /pmc/articles/PMC9289263/ /pubmed/35860466 http://dx.doi.org/10.3389/fgene.2022.831452 Text en Copyright © 2022 Mannens, Lombardi, Alders, Henneman and Bliek. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Mannens, M. M. A. M.
Lombardi, M. P.
Alders, M.
Henneman, P.
Bliek, J.
Further Introduction of DNA Methylation (DNAm) Arrays in Regular Diagnostics
title Further Introduction of DNA Methylation (DNAm) Arrays in Regular Diagnostics
title_full Further Introduction of DNA Methylation (DNAm) Arrays in Regular Diagnostics
title_fullStr Further Introduction of DNA Methylation (DNAm) Arrays in Regular Diagnostics
title_full_unstemmed Further Introduction of DNA Methylation (DNAm) Arrays in Regular Diagnostics
title_short Further Introduction of DNA Methylation (DNAm) Arrays in Regular Diagnostics
title_sort further introduction of dna methylation (dnam) arrays in regular diagnostics
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9289263/
https://www.ncbi.nlm.nih.gov/pubmed/35860466
http://dx.doi.org/10.3389/fgene.2022.831452
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